Hao Deng

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 18

Top Venues

Journal of cellular and molecular medicine

Bioscience reports

Molecular genetics & genomic medicine

Journal of ophthalmology

Central South University

Xiangya School of Medicine, Central South University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Central South University

China

Professor, Doctoral supervisor

Central South University

China

Professor

Baylor College of Medicine Sep 01 2006 - Aug 30 2007

United States

Instructor (faculty)

Central South University Sep 01 2002 - Jan 27 2004

China

Instructor

Central South University Sep 01 2000 - Aug 30 2002

China

Research Associate

Hunan Medical University Jul 01 1995 - Aug 30 1997

China

Research Assistant

Education History

Xiangya School of Medicine, Central South University Sep 01 2000 - Jun 30 2003

China

PHD

Xiangya School of Medicine, Central South University Sep 01 1997 - Jul 01 2000

China

MSC

Publications

Lamei Yuan, Ruikang Yang, Hao Deng
Auricular fistula: a review of its clinical manifestations, genetics, and treatments. Journal of molecular medicine (Berlin, Germany) (2023)
Ying Xiong, Hong Xia, Lamei Yuan, Sheng Deng, Zerui Ding, Hao Deng
Identification of compound heterozygous DNAH11 variants in a Han-Chinese family with primary ciliary dyskinesia. Journal of cellular and molecular medicine 25 (18) (2021)
Qin Xiang, Yanna Cao, Hongbo Xu, Zhijian Yang, Liang Tang, Ju Xiang, Jianming Li, Hao Deng, Lamei Yuan
Novel MFSD8 Variants in a Chinese Family with Nonsyndromic Macular Dystrophy. Journal of ophthalmology 2021 (2021)
Hong Xia, Xiangjun Huang, Sheng Deng, Hongbo Xu, Yan Yang, Xin Liu, Lamei Yuan, Hao Deng
DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease. PloS one 16 (6) (2021)
Hao Deng, Xue Yan, Lamei Yuan
Human genetic basis of coronavirus disease 2019. Signal transduction and targeted therapy 6 (1) (2021)
Wenmiao Liu, Yixia Guo, Xiumei Liu, Ru Zhang, Jicheng Dong, Hao Deng, Fan He, Fengyuan Che, Shiguo Liu, Mingji Yi
Family-Based Analysis Combined with Case-Controls Study Implicate Roles of PCNT in Tourette Syndrome. Neuropsychiatric disease and treatment 16 (2020)
Yuan Wu, Yi Guo, Junhui Yi, Hongbo Xu, Lamei Yuan, Zhijian Yang, Hao Deng
Heterozygous RHO p.R135W missense mutation in a large Han-Chinese family with retinitis pigmentosa and different refractive errors. Bioscience reports 39 (7) (2019)
Hao Deng, Shan Wu, Joseph Jankovic
[Essential tremor: genetic update]. Expert reviews in molecular medicine 21 (2019)
Qin Xiang, Lamei Yuan, Yanna Cao, Hongbo Xu, Yunfeiyang Li, Hao Deng
Identification of a Heterozygous Mutation in the TGFBI Gene in a Hui-Chinese Family with Corneal Dystrophy. Journal of ophthalmology 2019 (2019)
Mingyuan Wang, Yi Guo, Pengfei Rong, Hongbo Xu, Lina Gong, Hao Deng, Lamei Yuan
COL1A2 p.Gly1066Val variant identified in a Han Chinese family with osteogenesis imperfecta type I. Molecular genetics & genomic medicine 7 (5) (2019)
Yi Guo, Peng Wang, Xiaorong Li, Shaihong Zhu, Hongbo Xu, Shizhou Li, Hao Deng, Lamei Yuan
Identifying a BRCA2 c.5722_5723del mutation in a Han-Chinese family with breast cancer. Bioscience reports 39 (4) (2019)
Kuan Fan, Pengzhi Hu, Chengyuan Song, Xiong Deng, Jie Wen, Yi-Ming Liu, Hao Deng
Novel Compound Heterozygous PRKN Variants in a Han-Chinese Family with Early-Onset Parkinson's Disease. Parkinson's disease 2019 (2019)
Xiangjun Huang, Yi Guo, Hongbo Xu, Zhijian Yang, Xiong Deng, Hao Deng, Lamei Yuan
Identification of a novel EVC variant in a Han-Chinese family with Ellis-van Creveld syndrome. Molecular genetics & genomic medicine 7 (9) (2019)
Yuan Wu, Lamei Yuan, Yi Guo, Anjie Lu, Wen Zheng, Hongbo Xu, Yan Yang, Pengzhi Hu, Shaojuan Gu, Bingqi Wang, Hao Deng
Identification of a GNE homozygous mutation in a Han-Chinese family with GNE myopathy. Journal of cellular and molecular medicine 22 (11) (2018)
Kuan Fan, Haixia Zhu, Hongbo Xu, Ping Mao, Lamei Yuan, Hao Deng
The identification of a transthyretin variant p.D38G in a Chinese family with early-onset leptomeningeal amyloidosis. Journal of neurology 266 (1) (2018)
Heng Xiao, Xiangjun Huang, Hongbo Xu, Xiang Chen, Wei Xiong, Zhijian Yang, Xiong Deng, Zhenghao He, Hao Deng
A novel splice-site mutation in the ATP2C1 gene of a Chinese family with Hailey-Hailey disease. Journal of cellular biochemistry 120 (3) (2018)
Heng Xiao, Lamei Yuan, Hongbo Xu, Zhijian Yang, Feizhou Huang, Zhi Song, Yan Yang, Cheng Zeng, Hao Deng
Novel and Recurring Disease-Causing NF1 Variants in Two Chinese Families with Neurofibromatosis Type 1. Journal of molecular neuroscience : MN 65 (4) (2018)
Lamei Yuan, Xiong Deng, Zhi Song, Sheng Deng, Wen Zheng, Ping Mao, Hao Deng
Systematic analysis of genetic variants in patients with essential tremor. Brain and behavior 8 (10) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Hao Deng